{{Rsnum
|rsid=2517713
|Gene=HCP5P3
|Chromosome=6
|position=29950322
|Orientation=minus
|GMAF=0.3237
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 39.6 | 49.5 | 10.8
| HCB | 40.0 | 51.1 | 8.9
| JPT | 86.6 | 13.4 | 0.0
| YRI | 31.0 | 51.7 | 17.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 40.0 | 51.1 | 8.9
| CHD | 38.1 | 53.3 | 8.6
| GIH | 27.1 | 44.8 | 28.1
| LWK | 53.3 | 36.2 | 10.5
| MEX | 0.0 | 0.0 | 0.0
| MKK | 40.0 | 49.3 | 10.7
| TSI | 41.4 | 49.5 | 9.1
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19664746
|Trait=Nasopharyngeal Carcinoma
|Title=Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21.
|RiskAllele=A
|Pval=4E-20
|OR=1.88
|ORtxt=[1.65-2.15]
|OA=1
}}

{{omim
|id=161550
|rsnum=2517713
}}

{{PMID|18519066|OA=1
}} Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.

{{PMID|21283797|OA=1
}} Identification of genes with allelic imbalance on 6p associated with nasopharyngeal carcinoma in southern Chinese.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2517713
|overall_frequency_n=73
|overall_frequency_d=126
|overall_frequency=0.579365
|n_genomes=36
|n_genomes_annotated=0
|n_haplomes=56
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}